P
US9309320B2ActiveUtilityPatentIndex 49

Neutralization of CD95 activity blocks invasion of glioblastoma cells in vivo

Assignee: MARTIN-VILLALBA ANAPriority: Dec 28, 2006Filed: Dec 28, 2007Granted: Apr 12, 2016
Est. expiryDec 28, 2026(~0.5 yrs left)· nominal 20-yr term from priority
Inventors:MARTIN-VILLALBA ANAKLEBER SUSANNEWIESTLER BENEDIKTKRAMMER PETER GHEROLD-MENDE CHRISTELSANCHO-MARTINEZ IGNACIO
A61P 35/00G01N 33/57557C07K 16/2875G01N 2333/70578C07K 2319/30G01N 33/6863C07K 2317/76G01N 2510/00C07K 14/70575G01N 2500/04G01N 33/566A61K 38/00A61K 2039/505G01N 2500/00C07K 2319/00C07K 14/70578G01N 2500/10C07K 16/2878G01N 33/57407
49
PatentIndex Score
2
Cited by
30
References
6
Claims

Abstract

The present invention relates to methods for treating an individual with high grade glioblastoma multiforme by preventing or disrupting the binding of CD95 to its ligand, CD95L, in vivo, whereupon that neutralization of CD95 activity reduces undesirable glial cell migration and invasion into body tissue.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
       1. A method for treating an individual with high grade glioma, comprising administering an agent that neutralizes CD95 activity to an individual with high grade glioma, wherein said agent is a CD95 ligand (CD95L) inhibitor comprising
 a fusion protein comprising the extracellular domain of CD95 and a human Fc domain. 
 
     
     
       2. The method of  claim 1 , wherein the fusion protein is a fusion protein of the extracellular domain of the human CD95 with human IgG1-Fc (APG101). 
     
     
       3. The method of  claim 1 , wherein the high grade glioma is a WHO Grade III or IV glioma. 
     
     
       4. The method of  claim 1 , wherein the high grade glioma is a WHO Grade IV glioma. 
     
     
       5. The method of  claim 1 , wherein an interaction between CD95 and the protein p85 of PI3K is inhibited. 
     
     
       6. The method according to of  claim 1 , wherein said agent is administered in an amount sufficient to reduce glial cell migration and/or invasion.

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